Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut Microbiota

Glucosamine (GlcN) is used as a supplement for arthritis and joint pain and has been proved to have effects on inflammation, cancer, and cardiovascular diseases. However, there are limited studies on the regulatory mechanism of GlcN against glucose and lipid metabolism disorder. In this study, we tr...

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Main Authors: Xubing Yuan, Junping Zheng, Lishi Ren, Siming Jiao, Cui Feng, Yuguang Du, Hongtao Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-06-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2021.694107/full
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spelling doaj-268f9eacc39643fc9b3a1cdaf898b2a92021-06-03T05:31:56ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-06-011210.3389/fphar.2021.694107694107Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut MicrobiotaXubing Yuan0Xubing Yuan1Junping Zheng2Junping Zheng3Lishi Ren4Siming Jiao5Cui Feng6Yuguang Du7Hongtao Liu8State Key Laboratory of Biochemical Engineering and Key Laboratory of Biopharmaceutical Production and Formulation Engineering, PLA, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, ChinaInstitute of Process Engineering, University of Chinese Academy of Sciences, Beijing, ChinaState Key Laboratory of Biochemical Engineering and Key Laboratory of Biopharmaceutical Production and Formulation Engineering, PLA, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, ChinaInstitute of Process Engineering, University of Chinese Academy of Sciences, Beijing, ChinaState Key Laboratory of Biochemical Engineering and Key Laboratory of Biopharmaceutical Production and Formulation Engineering, PLA, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, ChinaState Key Laboratory of Biochemical Engineering and Key Laboratory of Biopharmaceutical Production and Formulation Engineering, PLA, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, ChinaState Key Laboratory of Biochemical Engineering and Key Laboratory of Biopharmaceutical Production and Formulation Engineering, PLA, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, ChinaState Key Laboratory of Biochemical Engineering and Key Laboratory of Biopharmaceutical Production and Formulation Engineering, PLA, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, ChinaState Key Laboratory of Biochemical Engineering and Key Laboratory of Biopharmaceutical Production and Formulation Engineering, PLA, Institute of Process Engineering, Chinese Academy of Sciences, Beijing, ChinaGlucosamine (GlcN) is used as a supplement for arthritis and joint pain and has been proved to have effects on inflammation, cancer, and cardiovascular diseases. However, there are limited studies on the regulatory mechanism of GlcN against glucose and lipid metabolism disorder. In this study, we treated high-fat diet (HFD)-induced diabetic mice with GlcN (1 mg/ml, in drinking water) for five months. The results show that GlcN significantly reduced the fasting blood glucose of HFD-fed mice and improved glucose tolerance. The feces of intestinal contents in mice were analyzed using 16s rDNA sequencing. It was indicated that GlcN reversed the imbalanced gut microbiota in HFD-fed mice. Based on the PICRUSt assay, the signaling pathways of glucolipid metabolism and biosynthesis were changed in mice with HFD feeding. By quantitative real-time PCR (qPCR) and hematoxylin and eosin (H&E) staining, it was demonstrated that GlcN not only inhibited the inflammatory responses of colon and white adipose tissues, but also improved the intestinal barrier damage of HFD-fed mice. Finally, the correlation analysis suggests the most significantly changed intestinal bacteria were positively or negatively related to the occurrence of inflammation in the colon and fat tissues of HFD-fed mice. In summary, our studies provide a theoretical basis for the potential application of GlcN to glucolipid metabolism disorder through the regulation of gut microbiota.https://www.frontiersin.org/articles/10.3389/fphar.2021.694107/fullglucosaminegut microbiotadiabetes mellitusinflammationhigh fat diet
collection DOAJ
language English
format Article
sources DOAJ
author Xubing Yuan
Xubing Yuan
Junping Zheng
Junping Zheng
Lishi Ren
Siming Jiao
Cui Feng
Yuguang Du
Hongtao Liu
spellingShingle Xubing Yuan
Xubing Yuan
Junping Zheng
Junping Zheng
Lishi Ren
Siming Jiao
Cui Feng
Yuguang Du
Hongtao Liu
Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut Microbiota
Frontiers in Pharmacology
glucosamine
gut microbiota
diabetes mellitus
inflammation
high fat diet
author_facet Xubing Yuan
Xubing Yuan
Junping Zheng
Junping Zheng
Lishi Ren
Siming Jiao
Cui Feng
Yuguang Du
Hongtao Liu
author_sort Xubing Yuan
title Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut Microbiota
title_short Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut Microbiota
title_full Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut Microbiota
title_fullStr Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut Microbiota
title_full_unstemmed Glucosamine Ameliorates Symptoms of High-Fat Diet-Fed Mice by Reversing Imbalanced Gut Microbiota
title_sort glucosamine ameliorates symptoms of high-fat diet-fed mice by reversing imbalanced gut microbiota
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2021-06-01
description Glucosamine (GlcN) is used as a supplement for arthritis and joint pain and has been proved to have effects on inflammation, cancer, and cardiovascular diseases. However, there are limited studies on the regulatory mechanism of GlcN against glucose and lipid metabolism disorder. In this study, we treated high-fat diet (HFD)-induced diabetic mice with GlcN (1 mg/ml, in drinking water) for five months. The results show that GlcN significantly reduced the fasting blood glucose of HFD-fed mice and improved glucose tolerance. The feces of intestinal contents in mice were analyzed using 16s rDNA sequencing. It was indicated that GlcN reversed the imbalanced gut microbiota in HFD-fed mice. Based on the PICRUSt assay, the signaling pathways of glucolipid metabolism and biosynthesis were changed in mice with HFD feeding. By quantitative real-time PCR (qPCR) and hematoxylin and eosin (H&E) staining, it was demonstrated that GlcN not only inhibited the inflammatory responses of colon and white adipose tissues, but also improved the intestinal barrier damage of HFD-fed mice. Finally, the correlation analysis suggests the most significantly changed intestinal bacteria were positively or negatively related to the occurrence of inflammation in the colon and fat tissues of HFD-fed mice. In summary, our studies provide a theoretical basis for the potential application of GlcN to glucolipid metabolism disorder through the regulation of gut microbiota.
topic glucosamine
gut microbiota
diabetes mellitus
inflammation
high fat diet
url https://www.frontiersin.org/articles/10.3389/fphar.2021.694107/full
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